Linked Data
dbSNP Id:
rs1708202674
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445556_15445557insC , CM000663.2:g.15445556_15445557insC | GRCh38 |
| NC_000001.10:g.15772051_15772052insC , CM000663.1:g.15772051_15772052insC | GRCh37 |
| NC_000001.9:g.15644638_15644639insC | NCBI36 |
| NG_009253.1:g.12114_12115insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.640-41_640-40insC MANE Select | ENSP00000365116.4:n.640-41_640-40insC | |
| ENST00000375943.6:c.*94-41_*94-40insC | ENSP00000365110.2:n.*94-41_*94-40insC | |
| ENST00000375949.4:c.640-41_640-40insC | ENSP00000365116.4:n.640-41_640-40insC | |
| ENST00000483406.1:n.404-41_404-40insC | ||
| NM_007272.2:c.640-41_640-40insC | NP_009203.2:n.640-41_640-40insC | |
| XM_011540550.1:c.494-41_494-40insC | XP_011538852.1:n.494-41_494-40insC | |
| NM_007272.3:c.640-41_640-40insC MANE Select | NP_009203.2:n.640-41_640-40insC |